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儿茶酚-O-甲基转移酶(Val158Met)基因多态性与西班牙人群中的神经性疼痛无关。

COMT (Val158Met) polymorphism is not associated to neuropathic pain in a Spanish population.

作者信息

Armero Pilar, Muriel Clemente, Santos Juan, Sànchez-Montero F J, Rodríguez Raquel E, González-Sarmiento Rogelio

机构信息

Unidad de Medicina Molecular, Departamento de Medicina, Universidad de Salamanca, Spain.

出版信息

Eur J Pain. 2005 Jun;9(3):229-32. doi: 10.1016/j.ejpain.2004.06.005.

Abstract

It is well known that the response to painful stimuli varies between individuals and this could be consequence of individual differences to pain sensitivity that may be related to genetic factors. Catechol-O-methyltransferase (COMT) is one of the enzymes that metabolize catecholamine neurotransmitters. Differences in the activity of COMT influence the functions of these neurotransmitters. A single nucleotide polymorphism (Val158Met) of COMT leads to a three to four fold reduction in the activity of the enzyme and has been associated to modifications in the response to a pain stressor. Neuropathic pain is a progressive nervous system disease due to an alteration of the peripheral or central nervous system. To elucidate the possible role of COMT polymorphism in the susceptibility to neuropathic pain, we have performed a case-control study in a Spanish population. Analysis of the (Val158Met) COMT polymorphism was performed by PCR amplification and DNA digestion with restriction enzymes. Our study concludes that functional Val158Met polymorphism of COMT gene is not associated to increased susceptibility to neuropathic pain.

摘要

众所周知,个体对疼痛刺激的反应存在差异,这可能是个体对疼痛敏感性存在差异的结果,而这种差异可能与遗传因素有关。儿茶酚-O-甲基转移酶(COMT)是代谢儿茶酚胺神经递质的酶之一。COMT活性的差异会影响这些神经递质的功能。COMT的单核苷酸多态性(Val158Met)会导致该酶的活性降低三到四倍,并与疼痛应激源反应的改变有关。神经性疼痛是一种由于外周或中枢神经系统改变而导致的进行性神经系统疾病。为了阐明COMT多态性在神经性疼痛易感性中的可能作用,我们在西班牙人群中进行了一项病例对照研究。通过PCR扩增和限制性酶切对COMT(Val158Met)多态性进行分析。我们的研究得出结论,COMT基因的功能性Val158Met多态性与神经性疼痛易感性增加无关。

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